http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103941020-B

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-285
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-6803
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-56911
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-68
filingDate 2014-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2016-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103941020-B
titleOfInvention A kind of indirect ELISA reagent kit detecting haemophilus parasuis antibody
abstract The invention discloses a kind of indirect ELISA reagent kit detecting haemophilus parasuis antibody.Is this kit by haemophilus parasuis cell lethality expansion toxin C (cytolethal? distending? toxin, CDT-C) albumen assembles by plate, measuring samples dilution plate, positive control serum, negative control sera, 20 times of concentrated cleaning solutions, serum sample dilution, enzyme labelled antibody working fluid, nitrite ion and stop buffers as the ELISA bag of envelope antigen.Criterion: S/P value & lt; 0.200, be judged to feminine gender; S/P value >=0.200, is judged to the positive, S/P value=(sample to be tested OD450nm average-negative control OD450nm average)/(positive sample OD450nm average-negative control OD450nm average).By specific test, sensitivity tests, replica test, coincidence rate test, with listing kit comparison test, clinical practice test etc., show that this kit has the features such as specificity is good, susceptibility is high, reproducible, with external similar commercialized product, there is higher coincidence rate, can be used for clinical extensive detection and the epidemiology survey of haemophilus parasuis antibody.
priorityDate 2014-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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